Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) VED-220Recalls & reported problems
Xeridiem Medical Devices, Inc. · Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) 20FR · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813939024944), received between Mar 13, 2020 and Mar 13, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Migration1
Patient problems
- Abdominal Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 13, 2020Migration; Migration
THE DEVICE WAS IN PLACE FOR LESS THAN A MONTH WHEN IT TRAVELED INTO THE PATIENT'S DUODENUM DURING NORMAL DAILY ROUTINES. CAREGIVER INDICATED THAT PATIENT IS PRETTY IMMOBILE AND MOVES FROM BED TO WHEELCHAIR DAILY. SHE INDICATED THE BUMPER IS LOOSE TO PAST G-TUBES THEY HAVE USED. USER VOLUNTARY MEDWATCH REPORT MW5092795 WAS RECEIVED AND FURTHER INDICATED THAT PATIENT PRESENTED TO ER WITH ABDOMINAL PAIN, UNABLE TO TOLERATE ENTERAL FEEDING. PATIENT WAS WITHOUT NUTRITION FOR 2 DAYS AT TIME OF DEVICE REMOVAL. DEVICE HAD PASSED INTO DUODENUM AND WAS CAUSING BLOCKAGE.
Patient problems: Abdominal Pain
MAUDE report 9832248 ↗
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- EndoVive Standard PEG Kit M00509050Boston Scientific Corporation · Gastrointestinal Tubes with Enteral Specific Connectors1 recall6 reports
- Salem Sump 8888264986ECardinal Health 200, LLC · Gastrointestinal Tubes with Enteral Specific Connectors1 recall1 death2 reports
- Salem Sump 8888268060ECardinal Health 200, LLC · Gastrointestinal Tubes with Enteral Specific Connectors1 recall0 reports
- Salem Sump 7771810ECardinal Health, Inc. · Gastrointestinal Tubes with Enteral Specific Connectors28 reports
- Salem Sump 7771610ECardinal Health, Inc. · Gastrointestinal Tubes with Enteral Specific Connectors1 death18 reports
- Edi Catheter ENFit 6Fr/49 cm, 5pcs 6883898Maquet Critical Care AB · Gastrointestinal Tubes With Enteral Specific Connectors14 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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